Publications by authors named "Ertl D"

Predicting phenotypes from a combination of genetic and environmental factors is a grand challenge of modern biology. Slight improvements in this area have the potential to save lives, improve food and fuel security, permit better care of the planet, and create other positive outcomes. In 2022 and 2023 the first open-to-the-public Genomes to Fields (G2F) initiative Genotype by Environment (GxE) prediction competition was held using a large dataset including genomic variation, phenotype and weather measurements and field management notes, gathered by the project over nine years.

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  • - Predicting how genetic and environmental factors influence traits (phenotypes) is a critical challenge in biology, with potential benefits like improved health, food security, and environmental care.
  • - The Genomes to Fields (G2F) initiative hosted a competition in 2022 and 2023, inviting global participants from various disciplines to develop models using a comprehensive dataset gathered over nine years, including genetic and environmental data.
  • - Winning methods combined machine learning with traditional breeding techniques, showcasing a variety of approaches such as quantitative genetics and deep learning, indicating that no single strategy was universally superior in predicting phenotypes in this context.
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  • The study compared the effects of growth hormone therapy on children with growth hormone deficiency (GHD) and those born small for their gestational age (SGA), revealing significant differences in growth outcomes.
  • After one year of therapy, children with GHD showed a greater increase in height compared to those with SGA, and this trend continued at their final height.
  • The research indicated that short-term height increases were predictive of long-term growth outcomes in GHD patients, but not in SGA patients, suggesting differing responses to growth hormone therapy between these groups.
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  • The paper emphasizes the need for simultaneous advancements in genomics (measuring genetic variation) and phenomics (measuring trait variation) for agricultural populations to improve agricultural productivity.
  • It discusses the Agricultural Genome to Phenome Initiative (AG2PI) and its efforts to coordinate with government agencies and stakeholders to improve agricultural outcomes through research collaboration.
  • A workshop was held to identify challenges and innovation opportunities in AG2P research, resulting in a vision for future advancements and six specific goals for immediate implementation.
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Objectives: The aim of this project was to develop a rectal formulation of metyrapone suitable for application in an infant hospitalised with McCune-Albright syndrome (MAS)-related Cushing syndrome and to provide a detailed description of the formulation protocol including quality control parameters.

Methods: Suppositories with a drug load of up to 100 mg metyrapone were prepared. Mass variation, content uniformity and drug release were analysed according to the guidelines set out by the European Pharmacopoeia.

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A female toddler was diagnosed at age ten months with peripheral precocious puberty and hypercortisolism related to McCune Albright Syndrome with additional systemic complications. We present the first successful, long-term use of metyrapone as suppositories, with striking clinical and biochemical improvement and no side-effects.

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  • - This study aimed to analyze the final height (FH) trends in French patients with X-linked hypophosphatemia (XLH) over the past decades, as there was limited data on FH's natural history in this condition.
  • - Researchers conducted a retrospective study involving 398 XLH patients, dividing them into three birth groups (1950-1974, 1975-2000, and 2001-2006) to compare their average final heights.
  • - Results showed a significant increase in mean FH over the generations, with men still being shorter than women, indicating ongoing challenges in treating XLH. Despite improvements, many patients continue to have short stature, highlighting the need for continued progress.
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  • - The Maize GxE project, part of the Genomes to Fields Initiative, studies how different genetic types (genotypes) of maize interact with varying environmental conditions to improve resource use and predictability in crop performance.
  • - Data collected from 30 locations in the US and one in Germany during 2020-2021 include phenotypic details, soil and climate measurements, and other relevant metadata, all of which are being made publicly accessible.
  • - Collaborators at each site collected and submitted data, which was then verified and compiled by a coordination team, ensuring accuracy before releasing a minimally filtered version to the public.
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Objectives: The Genomes to Fields (G2F) 2022 Maize Genotype by Environment (GxE) Prediction Competition aimed to develop models for predicting grain yield for the 2022 Maize GxE project field trials, leveraging the datasets previously generated by this project and other publicly available data.

Data Description: This resource used data from the Maize GxE project within the G2F Initiative [1]. The dataset included phenotypic and genotypic data of the hybrids evaluated in 45 locations from 2014 to 2022.

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  • Maternal inactivating GNAS mutations cause pseudohypoparathyroidism 1A (PHP1A), leading to growth issues, hormone resistance, and other physical symptoms in affected individuals.
  • A study examined the effects of recombinant human growth hormone (rhGH) on growth in 190 patients, comparing those who received treatment to untreated controls to evaluate height outcomes.
  • Results showed that rhGH significantly improved height in treated patients after 1 and 3 years, highlighting its potential benefits, but further research is needed to ensure long-term safety and effectiveness.
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Objectives: This report provides information about the public release of the 2018-2019 Maize G X E project of the Genomes to Fields (G2F) Initiative datasets. G2F is an umbrella initiative that evaluates maize hybrids and inbred lines across multiple environments and makes available phenotypic, genotypic, environmental, and metadata information. The initiative understands the necessity to characterize and deploy public sources of genetic diversity to face the challenges for more sustainable agriculture in the context of variable environmental conditions.

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Background: Achondroplasia, caused by a pathogenic variant in the fibroblast growth factor receptor 3 gene, is the most common skeletal dysplasia. The Lifetime Impact of Achondroplasia Study in Europe (LIAISE; NCT03449368) aimed to quantify the burden of achondroplasia among individuals across a broad range of ages, including adults.

Methods: Demographic, clinical and healthcare resource use data were collected from medical records of achondroplasia patients enrolled in 13 sites across six European countries in this retrospective, observational study.

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Introduction: Severe short stature is a feature of acrodysostosis, but data on growth are sparse. Treatment with recombinant human growth hormone (rhGH) is used in some centers to increase final height, but no studies have been published so far. Our objective was to conduct a multicenter, retrospective, cohort study to investigate growth in individuals with both types of acrodysostosis, treated with rhGH or not; we used the new nomenclature to describe acrodysostosis, as this disease belongs to the large group of inactivating PTH/PTHrP signaling disorders (iPPSD); acrodysostosis refers to iPPSD4 (acrodysostosis type 1 due to PRKAR1A mutations) and iPPSD5 (acrodysostosis type 2, due to PDE4D mutations).

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Accurate prediction of the phenotypic outcomes produced by different combinations of genotypes, environments, and management interventions remains a key goal in biology with direct applications to agriculture, research, and conservation. The past decades have seen an expansion of new methods applied toward this goal. Here we predict maize yield using deep neural networks, compare the efficacy of 2 model development methods, and contextualize model performance using conventional linear and machine learning models.

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  • X-linked hypophosphatemia (XLH) leads to issues like increased FGF23, low phosphate levels, and growth problems, but treatments like vitamin D supplements, phosphate, and rhGH are used to improve outcomes.
  • A study involving 36 patients showed limited height improvements in those treated with burosumab alone, while those on combined rhGH and burosumab therapies experienced continued height gains.
  • The research is significant as it’s one of the largest in Europe, indicating that combining rhGH with burosumab appears safe and may enhance growth in children with XLH.
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Hypophosphatasia (HPP) is an inborn error of metabolism caused by loss-of-function mutations in the biomineralization-associated alkaline phosphatase gene, encoding tissue-nonspecific alkaline phosphatase (TNSALP). Symptoms include skeletal hypomineralization and extra-skeletal manifestations such as pyridoxine (B6)-responsive seizures due to impaired cerebral B6 passage. Since the introduction of enzyme replacement therapy (ERT), skeletal manifestations and B6-responsive seizures were reported to improve significantly.

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Genomic prediction provides an efficient alternative to conventional phenotypic selection for developing improved cultivars with desirable characteristics. New and improved methods to genomic prediction are continually being developed that attempt to deal with the integration of data types beyond genomic information. Modern automated weather systems offer the opportunity to capture continuous data on a range of environmental parameters at specific field locations.

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High-dimensional and high-throughput genomic, field performance, and environmental data are becoming increasingly available to crop breeding programs, and their integration can facilitate genomic prediction within and across environments and provide insights into the genetic architecture of complex traits and the nature of genotype-by-environment interactions. To partition trait variation into additive and dominance (main effect) genetic and corresponding genetic-by-environment variances, and to identify specific environmental factors that influence genotype-by-environment interactions, we curated and analyzed genotypic and phenotypic data on 1918 maize (Zea mays L.) hybrids and environmental data from 65 testing environments.

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Diagnosing and treating hypercalcemia during pregnancy can be challenging due to both the physiological changes in calcium homeostasis and the underlying cause for the hypercalcemia. During pregnancy and lactation there is increased mobilization of calcium in the mother to meet the fetus' calcium requirements. Here we discuss the diagnostic challenges, management, and patient perspective of hypercalcemia during pregnancy in two particular cases and in other rare conditions causing hypercalcemia.

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The heterogeneity of "rare bone disorders" can be explained by the number of molecules and regulatory pathways which are responsible for bone health and normal stature. In this article, the most important basic principles behind bone homeostasis from development to structure and regulation of the growing skeleton are summarized. The aim is to provide the reader with some theoretical background to understand the nature of the different main groups of disorders affecting bone stability, longitudinal growth and disturbances of calcium and phosphate homeostasis.

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Objective: Young women with Turner syndrome (TS) are known to be at risk for loss to medical follow-up. Recent literature indicates that there are disparities regarding transition readiness between different chronic conditions. So far, studies in young women with TS investigating their transition readiness compared to youths with other chronic conditions with no or minor neurocognitive challenges have not been reported.

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  • The study investigates the role of serum acid-labile subunit (ALS) as a potential biomarker for diagnosing growth hormone deficiency (GHD) in children, alongside standard markers IGF-I and IGFBP-3.
  • Ninety-one children undergoing GHD diagnosis were analyzed, revealing that IGF-I was the most significant predictor of GHD, with ALS contributing little to the diagnosis.
  • The findings conclude that measuring ALS, whether alone or with other biomarkers, does not improve the detection of GHD compared to using IGF-I and IGFBP-3, which performed similarly in diagnostic accuracy.
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